Nandrolone phenpropionate (BioDeep_00000006675)

 

Secondary id: BioDeep_00001868156

human metabolite blood metabolite Chemicals and Drugs


代谢物信息卡片


(1S,2R,10R,11S,14S,15S)-15-methyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-yl 3-phenylpropanoate

化学式: C27H34O3 (406.25078140000005)
中文名称: 苯丙酸诺龙
谱图信息: 最多检出来源 Homo sapiens(blood) 30.77%

分子结构信息

SMILES: CC12CCC3C(C1CCC2OC(=O)CCC4=CC=CC=C4)CCC5=CC(=O)CCC35
InChI: InChI=1S/C27H34O3/c1-27-16-15-22-21-11-9-20(28)17-19(21)8-10-23(22)24(27)12-13-25(27)30-26(29)14-7-18-5-3-2-4-6-18/h2-6,17,21-25H,7-16H2,1H3

描述信息

Nandrolone phenpropionate is only found in individuals that have used or taken this drug. It is a C18 steroid with androgenic and anabolic properties. It is generally prepared from alkyl ethers of estradiol to resemble testosterone but less one carbon at the 19 position. It is a schedule III drug in the U.S. Nandrolone is an androgen receptor agonist. The drug bound to the receptor complexes which allows it to enter the nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects.
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D045930 - Anabolic Agents
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

同义名列表

29 个代谢物同义名

(1S,2R,10R,11S,14S,15S)-15-methyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-yl 3-phenylpropanoate; 17 beta-Hydroxyestr-4-en-3-one hydrocinnamate; Nandrolone phenpropionate, (17alpha)-isomer; Norandrostenolone phenylpropionic acid; Nortestosterone phenylpropionic acid; Norandrolone phenyl propionic acid; Norandrostenolone phenylpropionate; Nortestosterone phenylpropionate; Nandrolone phenylpropionic acid; Nandrolon phenylpropionic acid; Norandrolone phenyl propionate; Nadrolone phenylpropionic acid; Norandrolone phenylpropionate; Testosterone Phenylpropionate; Nandrolone phenpropionic acid; Nandrolone phenylpionic acid; Nandrolone phenylpropionate; Nandrolon phenylpropionate; Nadrolone phenylpropionate; Nandrolone phenpropionate; Nandrolone phenylpionate; Nandrolin; Durabolin; Nerobolyl; Fenobolin; Nerobolil; 19NTPP; NTPP; NPP



数据库引用编号

18 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。



文献列表

  • Jasmine A Richman, Leah R Davis, Michael P Phelps. Gene Function is a Driver of Activin Signaling Pathway Evolution Following Whole-Genome Duplication in Rainbow Trout (Oncorhynchus mykiss). Genome biology and evolution. 2024 May; 16(5):. doi: 10.1093/gbe/evae096. [PMID: 38701021]
  • John D Griffin, Joanne M Buxton, Jeffrey A Culver, Robert Barnes, Emily A Jordan, Alexis R White, Stephen E Flaherty, Barbara Bernardo, Trenton Ross, Kendra K Bence, Morris J Birnbaum. Hepatic Activin E mediates liver-adipose inter-organ communication, suppressing adipose lipolysis in response to elevated serum fatty acids. Molecular metabolism. 2023 Dec; 78(?):101830. doi: 10.1016/j.molmet.2023.101830. [PMID: 38787338]
  • Huan Liu, Armen Yerevanian, Maria Westerhoff, Margaret H Hastings, Justin Ralph Baldovino Guerra, Meng Zhao, Katrin J Svensson, Bishuang Cai, Alexander A Soukas, Anthony Rosenzweig. Roles of Activin A and Gpnmb in metabolic dysfunction-associated steatotic liver disease (MASLD). Diabetes. 2023 Nov; ?(?):. doi: 10.2337/db23-0357. [PMID: 37934943]
  • Huan Liu, Margaret Hallauer Hastings, Robert Kitchen, Chunyang Xiao, Justin Ralph Baldovino Guerra, Alexandra Kuznetsov, Anthony Rosenzweig. Beneficial Effects of Moderate Hepatic Activin A Expression on Metabolic Pathways, Inflammation, and Atherosclerosis. Arteriosclerosis, thrombosis, and vascular biology. 2023 02; 43(2):330-349. doi: 10.1161/atvbaha.122.318138. [PMID: 36453275]
  • Jingjing Li, Letong Yin, Jingxiu Bi, David Stanley, Qili Feng, Qisheng Song. The TGF-β Receptor Gene Saxophone Influences Larval-Pupal-Adult Development in Tribolium castaneum. Molecules (Basel, Switzerland). 2022 Sep; 27(18):. doi: 10.3390/molecules27186017. [PMID: 36144752]
  • Excel R S Maylem, Leon J Spicer. Effects of transforming growth factor β1 on steroidogenesis of feline granulosa cells cultured in vitro. Reproduction, fertility, and development. 2022 Jul; 34(11):789-797. doi: 10.1071/rd22034. [PMID: 35605602]
  • Stanislas Bataille, Laetitia Dou, Marc Bartoli, Marion Sallée, Julien Aniort, Borhane Ferkak, Rania Chermiti, Nathalie McKay, Nathalie Da Silva, Stéphane Burtey, Stéphane Poitevin. Mechanisms of myostatin and activin A accumulation in chronic kidney disease. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 2022 06; 37(7):1249-1260. doi: 10.1093/ndt/gfac136. [PMID: 35333341]
  • Liqin Liu, Shijie Zhao, Zhenming Lü, Zan Pang, Bingjian Liu, Li Gong, Yinghui-Dong. Identification, expression and functional analysis of activin type I receptor in common Chinese Cuttlefish, Sepiella japonica. Animal reproduction science. 2022 May; 240(?):106976. doi: 10.1016/j.anireprosci.2022.106976. [PMID: 35439681]
  • Jun-Li Du, Feng Chen, Jian-Jian Wu, Lin Jin, Guo-Qing Li. Smad on X is vital for larval-pupal transition in a herbivorous ladybird beetle. Journal of insect physiology. 2022 May; 139(?):104387. doi: 10.1016/j.jinsphys.2022.104387. [PMID: 35367434]
  • Joan C Krepinsky. Activin B, a new player in kidney fibrosis?†. The Journal of pathology. 2022 04; 256(4):363-365. doi: 10.1002/path.5847. [PMID: 34882799]
  • Kelly L Walton, Monica P Goney, Zoe Peppas, Jessica M Stringer, Amy Winship, Karla Hutt, Georgia Goodchild, Shreya Maskey, Karen L Chan, Emilie Brûlé, Daniel J Bernard, William A Stocker, Craig A Harrison. Inhibin Inactivation in Female Mice Leads to Elevated FSH Levels, Ovarian Overstimulation, and Pregnancy Loss. Endocrinology. 2022 04; 163(4):. doi: 10.1210/endocr/bqac025. [PMID: 35255139]
  • Georgia P Wong, Faith Andres, Susan P Walker, Teresa M MacDonald, Ping Cannon, Tuong-Vi Nguyen, Emerson Keenan, Natalie J Hannan, Stephen Tong, Tu'uhevaha J Kaitu'u-Lino. Circulating Activin A is elevated at 36 weeks' gestation preceding a diagnosis of preeclampsia. Pregnancy hypertension. 2022 Mar; 27(?):23-26. doi: 10.1016/j.preghy.2021.11.006. [PMID: 34844073]
  • Szabina Szófia Szilágyi, Ayelet R Amsalem-Zafran, Keren E Shapira, Marcelo Ehrlich, Yoav I Henis. Competition between type I activin and BMP receptors for binding to ACVR2A regulates signaling to distinct Smad pathways. BMC biology. 2022 02; 20(1):50. doi: 10.1186/s12915-022-01252-z. [PMID: 35177083]
  • Andrew S Terker, T Alp Ikizler. Untangling the fibers of sarcopenia: activin A in chronic kidney disease-associated muscle wasting. Kidney international. 2022 02; 101(2):211-213. doi: 10.1016/j.kint.2021.08.034. [PMID: 34718004]
  • Tao Lin, Shanshan Wang, Stefan Munker, Kyounghwa Jung, Ricardo U Macías-Rodríguez, Astrid Ruiz-Margáin, Robert Schierwagen, Hui Liu, Chen Shao, Chunlei Fan, Rilu Feng, Xiaodong Yuan, Sai Wang, Franziska Wandrer, Christoph Meyer, Ralf Wimmer, Roman Liebe, Jens Kroll, Long Zhang, Tobias Schiergens, Peter Ten Dijke, Andreas Teufel, Alexander Marx, Peter R Mertens, Hua Wang, Matthias P A Ebert, Heike Bantel, Enrico N De Toni, Jonel Trebicka, Steven Dooley, Donghun Shin, Huiguo Ding, Hong-Lei Weng. Follistatin-controlled activin-HNF4α-coagulation factor axis in liver progenitor cells determines outcome of acute liver failure. Hepatology (Baltimore, Md.). 2022 02; 75(2):322-337. doi: 10.1002/hep.32119. [PMID: 34435364]
  • Elliot A Perens, Hal M Hoffman, Robert H Mak. Activin A Signaling Provides an Interorgan Link Between Kidney and Muscle in CKD-Associated Muscle Wasting. American journal of kidney diseases : the official journal of the National Kidney Foundation. 2022 02; 79(2):302-304. doi: 10.1053/j.ajkd.2021.09.007. [PMID: 34653537]
  • Pauline C Xu, Mikyoung You, Seok-Yeong Yu, Yi Luan, Maya Eldani, Thomas C Caffrey, Paul M Grandgenett, Kelly A O'Connell, Surendra K Shukla, Chandramohan Kattamuri, Michael A Hollingsworth, Pankaj K Singh, Thomas B Thompson, Soonkyu Chung, So-Youn Kim. Visceral adipose tissue remodeling in pancreatic ductal adenocarcinoma cachexia: the role of activin A signaling. Scientific reports. 2022 01; 12(1):1659. doi: 10.1038/s41598-022-05660-7. [PMID: 35102236]
  • Megan McAleavy, Qian Zhang, Peter J Ehmann, Jianing Xu, Matthew F Wipperman, Dharani Ajithdoss, Li Pan, Matthew Wakai, Raphael Simonson, Abhilash Gadi, Adelekan Oyejide, Sara C Hamon, Anita Boyapati, Lori G Morton, Tea Shavlakadze, Christos A Kyratsous, David J Glass. The Activin/FLRG Pathway Associates with Poor COVID-19 Outcomes in Hospitalized Patients. Molecular and cellular biology. 2022 01; 42(1):e0046721. doi: 10.1128/mcb.00467-21. [PMID: 34723652]
  • Sahar E M El-Deek, Sary K H Abd-Elghaffar, Randa S Hna, Heba G Mohamed, Heba E M El-Deek. Effect of Hesperidin against Induced Colon Cancer in Rats: Impact of Smad4 and Activin A Signaling Pathway. Nutrition and cancer. 2022; 74(2):697-714. doi: 10.1080/01635581.2021.1907424. [PMID: 33818196]
  • Rukmali Wijayarathna, Rosemary Genovese, Andreas Meinhardt, Kate L Loveland, Nigel P Groome, Barry T Hinton, Mark P Hedger. Examination of testicular lumicrine regulation of activins and immunoregulatory genes in the epididymal caput. Andrology. 2022 01; 10(1):190-201. doi: 10.1111/andr.13099. [PMID: 34415685]
  • Zhujun Yi, Shanqiao Wei, Lin Jin, Sivakumar Jeyarajan, Jing Yang, Yumei Gu, Hong Sun Kim, Shula Schechter, Shuang Lu, Michelle T Paulsen, Karan Bedi, Ishwarya Venkata Narayanan, Mats Ljungman, Howard C Crawford, Marina Pasca di Magliano, Kai Ge, Yali Dou, Jiaqi Shi. KDM6A Regulates Cell Plasticity and Pancreatic Cancer Progression by Noncanonical Activin Pathway. Cellular and molecular gastroenterology and hepatology. 2022; 13(2):643-667. doi: 10.1016/j.jcmgh.2021.09.014. [PMID: 34583087]
  • Nandor Barany, Anita Rozsas, Zsolt Megyesfalvi, Michael Grusch, Balazs Hegedus, Christian Lang, Kristiina Boettiger, Anna Schwendenwein, Anna Tisza, Ferenc Renyi-Vamos, Karin Schelch, Konrad Hoetzenecker, Mir Alireza Hoda, Sandor Paku, Viktoria Laszlo, Balazs Dome. Clinical relevance of circulating activin A and follistatin in small cell lung cancer. Lung cancer (Amsterdam, Netherlands). 2021 11; 161(?):128-135. doi: 10.1016/j.lungcan.2021.09.008. [PMID: 34583221]
  • Shih-Chen Chang, Chien-Yi Hsu, Li-Kuo Liu, Ya-Wen Lu, Yi-Lin Tsai, Ruey-Hsing Chou, Po-Hsun Huang, Liang-Kung Chen, Shing-Jong Lin. The association between serum activin A levels and albuminuria among community-dwelling middle-aged and older adults in Taiwan. Scientific reports. 2021 10; 11(1):20032. doi: 10.1038/s41598-021-99081-7. [PMID: 34625604]
  • Tian Xie, Lizhen Han, Yongxing Chen, Haihong Wu. Progranulin and Activin A Concentrations are Elevated in Serum from Patients with Acute Exacerbations of Idiopathic Pulmonary Fibrosis. Lung. 2021 10; 199(5):467-473. doi: 10.1007/s00408-021-00470-6. [PMID: 34462814]
  • Maíra Casalechi, Bruna B Coimbra, Débora M Rocha, Fernanda R Carvalho, Alessandra D Clarizia, Wiviane A Assis, Regina Amelia Lopes Pessoa Aguiar, Fernando M Reis. Serum and urine levels of activin A in primigravidae and multigravidae: a prospective cross-sectional study. Women & health. 2021 09; 61(8):745-750. doi: 10.1080/03630242.2021.1965693. [PMID: 34376125]
  • Pasquale Esposito, Daniela Verzola, Daniela Picciotto, Leda Cipriani, Francesca Viazzi, Giacomo Garibotto. Myostatin/Activin-A Signaling in the Vessel Wall and Vascular Calcification. Cells. 2021 08; 10(8):. doi: 10.3390/cells10082070. [PMID: 34440838]
  • Marc Paul O'Sullivan, Niamh Denihan, Klaudia Sikora, Mikael Finder, Caroline Ahearne, Gerard Clarke, Boubou Hallberg, Geraldine B Boylan, Deirdre M Murray. Activin A and Acvr2b mRNA from Umbilical Cord Blood Are Not Reliable Markers of Mild or Moderate Neonatal Hypoxic-Ischemic Encephalopathy. Neuropediatrics. 2021 08; 52(4):261-267. doi: 10.1055/s-0041-1725012. [PMID: 33706404]
  • Nikoleta Kostopoulou, Sofia Bellou, Eleni Bagli, Maria Markou, Eleftherios Kostaras, Marko Hyvönen, Yiannis Kalaidzidis, Angelos Papadopoulos, Varvara Chalmantzi, Athena Kyrkou, Ekaterini Panopoulou, Theodore Fotsis, Carol Murphy. Embryonic stem cells are devoid of macropinocytosis, a trafficking pathway for activin A in differentiated cells. Journal of cell science. 2021 07; 134(13):. doi: 10.1242/jcs.246892. [PMID: 34313314]
  • Witold Kędzierski, Sylwester Kowalik, Wioleta Mojsym, Iwona Janczarek, Ewelina Tkaczyk. Plasma Activin A and Decorin in Exercised Purebred Arabian Horses - Preliminary Study. Journal of equine veterinary science. 2021 07; 102(?):103638. doi: 10.1016/j.jevs.2021.103638. [PMID: 34119190]
  • Francesca Solagna, Caterina Tezze, Maja T Lindenmeyer, Shun Lu, Guochao Wu, Shuya Liu, Yu Zhao, Robert Mitchell, Charlotte Meyer, Saleh Omairi, Temel Kilic, Andrea Paolini, Olli Ritvos, Arja Pasternack, Antonios Matsakas, Dominik Kylies, Julian Schulze Zur Wiesch, Jan-Eric Turner, Nicola Wanner, Viji Nair, Felix Eichinger, Rajasree Menon, Ina V Martin, Barbara M Klinkhammer, Elion Hoxha, Clemens D Cohen, Pierre-Louis Tharaux, Peter Boor, Tammo Ostendorf, Matthias Kretzler, Marco Sandri, Oliver Kretz, Victor G Puelles, Ketan Patel, Tobias B Huber. Pro-cachectic factors link experimental and human chronic kidney disease to skeletal muscle wasting programs. The Journal of clinical investigation. 2021 06; 131(11):. doi: 10.1172/jci135821. [PMID: 34060483]
  • Giuseppe Cianciolo, Gaetano La Manna, Irene Capelli, Lorenzo Gasperoni, Andrea Galassi, Paola Ciceri, Mario Cozzolino. The role of activin: the other side of chronic kidney disease-mineral bone disorder?. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 2021 05; 36(6):966-974. doi: 10.1093/ndt/gfaa203. [PMID: 32940690]
  • Evgenia Synolaki, Vasileios Papadopoulos, Georgios Divolis, Olga Tsahouridou, Efstratios Gavriilidis, Georgia Loli, Ariana Gavriil, Christina Tsigalou, Nikolaos R Tziolos, Eleni Sertaridou, Bhanu Kalra, Ajay Kumar, Petros Rafailidis, Arja Pasternack, Dimitrios T Boumpas, Georgios Germanidis, Olli Ritvos, Simeon Metallidis, Panagiotis Skendros, Paschalis Sideras. The Activin/Follistatin Axis Is Severely Deregulated in COVID-19 and Independently Associated With In-Hospital Mortality. The Journal of infectious diseases. 2021 05; 223(9):1544-1554. doi: 10.1093/infdis/jiab108. [PMID: 33625513]
  • Cheng Yuan, Lihua Ni, Xiaoyan Wu. Activin A activation drives renal fibrosis through the STAT3 signaling pathway. The international journal of biochemistry & cell biology. 2021 05; 134(?):105950. doi: 10.1016/j.biocel.2021.105950. [PMID: 33609746]
  • Georgina Mancinelli, Carolina Torres, Nancy Krett, Jessica Bauer, Karla Castellanos, Ron McKinney, David Dawson, Grace Guzman, Rosa Hwang, Sam Grimaldo, Paul Grippo, Barbara Jung. Role of stromal activin A in human pancreatic cancer and metastasis in mice. Scientific reports. 2021 04; 11(1):7986. doi: 10.1038/s41598-021-87213-y. [PMID: 33846512]
  • Cecilia Veraar, Jonathan Kliman, Alberto Benazzo, Felicitas Oberndorfer, Maria Laggner, Philipp Hacker, Thomas Raunegger, Stefan Janik, Peter Jaksch, Walter Klepetko, Hendrik J Ankersmit, Bernhard Moser. Potential novel biomarkers for chronic lung allograft dysfunction and azithromycin responsive allograft dysfunction. Scientific reports. 2021 03; 11(1):6799. doi: 10.1038/s41598-021-85949-1. [PMID: 33762606]
  • Asfia Soomro, Jackie Trink, Kian O'Neil, Renzhong Li, Safaa Naiel, Bo Gao, Kjetil Ask, Joan C Krepinsky. Activin A and Cell-Surface GRP78 Are Novel Targetable RhoA Activators for Diabetic Kidney Disease. International journal of molecular sciences. 2021 Mar; 22(6):. doi: 10.3390/ijms22062839. [PMID: 33799579]
  • V K Chin, T H Tie, R Abd Majid, H Hassan, N Nordin, R Abas, R Basir. Inhibition of Activin A suppressed tumor necrosis factor-α secretion and improved histopathological conditions in malarial mice. Tropical biomedicine. 2021 Mar; 38(1):187-204. doi: 10.47665/tb.38.1.018. [PMID: 33797545]
  • Salah Aref, Lamiaa Ebrahim, Shaimaa El-Ashwah, Mohamed El Agdar, Mohamed Ayed. Relevance of plasma bone marrow Activin-A and CXCL-12 concentration levels as a biomarker in acute myeloid leukemia. Cancer biomarkers : section A of Disease markers. 2021; 32(3):263-270. doi: 10.3233/cbm-203171. [PMID: 34092614]
  • Shenglin Xian, Ang Chen, Xiaodan Wu, Chuanghong Lu, Yunjiao Wu, Feng Huang, Zhiyu Zeng. Activation of activin/Smad2 and 3 signaling pathway and the potential involvement of endothelial‑mesenchymal transition in the valvular damage due to rheumatic heart disease. Molecular medicine reports. 2021 01; 23(1):. doi: 10.3892/mmr.2020.11648. [PMID: 33179113]
  • Makoto Hashimoto, Gilbert Ho, Shuei Sugama, Takato Takenouchi, Masaaki Waragai, Hiromu Sugino, Satoshi Inoue, Eliezer Masliah. Possible Role of Activin in the Adiponectin Paradox-Induced Progress of Alzheimer's Disease. Journal of Alzheimer's disease : JAD. 2021; 81(2):451-458. doi: 10.3233/jad-210206. [PMID: 33814453]
  • Carmen Picón, Amalia Tejeda-Velarde, José Ignacio Fernández-Velasco, Manuel Comabella, Roberto Álvarez-Lafuente, Ester Quintana, Susana Sainz de la Maza, Enric Monreal, Noelia Villarrubia, José Carlos Álvarez-Cermeño, María Inmaculada Domínguez-Mozo, Lluís Ramió-Torrentà, Eulalia Rodríguez-Martín, Ernesto Roldán, Yolanda Aladro, Silvia Medina, Mercedes Espiño, Jaime Masjuan, Clara Matute-Blanch, Marta Muñoz-San Martín, Carmen Espejo, Carmen Guaza, Alfonso Muriel, Lucienne Costa-Frossard, Luisa María Villar. Identification of the Immunological Changes Appearing in the CSF During the Early Immunosenescence Process Occurring in Multiple Sclerosis. Frontiers in immunology. 2021; 12(?):685139. doi: 10.3389/fimmu.2021.685139. [PMID: 34322119]
  • Frédéric Vanhoutte, Su Liang, Marcella Ruddy, An Zhao, Tiera Drewery, Yuhuan Wang, Richard DelGizzi, Eduardo Forleo-Neto, Manoj Rajadhyaksha, Gary Herman, John D Davis. Pharmacokinetics and Pharmacodynamics of Garetosmab (Anti-Activin A): Results From a First-in-Human Phase 1 Study. Journal of clinical pharmacology. 2020 11; 60(11):1424-1431. doi: 10.1002/jcph.1638. [PMID: 32557665]
  • Zhipeng Cao, Irvin Jose, Jason Glab, Hamsa Puthalakath, Laura D Osellame, Nick J Hoogenraad. Generation of reporter cell lines for factors inducing muscle wasting in cancer cachexia. Analytical biochemistry. 2020 10; 606(?):113877. doi: 10.1016/j.ab.2020.113877. [PMID: 32738212]
  • Kai Chang, Ping Kang, Ying Liu, Kerui Huang, Ting Miao, Antonia P Sagona, Ioannis P Nezis, Rolf Bodmer, Karen Ocorr, Hua Bai. TGFB-INHB/activin signaling regulates age-dependent autophagy and cardiac health through inhibition of MTORC2. Autophagy. 2020 10; 16(10):1807-1822. doi: 10.1080/15548627.2019.1704117. [PMID: 31884871]
  • Penny A F Whiley, Liza O'Donnell, Sarah C Moody, David J Handelsman, Julia C Young, Elizabeth A Richards, Kristian Almstrup, Patrick S Western, Kate L Loveland. Activin A Determines Steroid Levels and Composition in the Fetal Testis. Endocrinology. 2020 07; 161(7):. doi: 10.1210/endocr/bqaa058. [PMID: 32274496]
  • Rui Liang, Xiaoxiao Xiao, Lilin Luo, Tianxing Chen, Hui Yang, Wanpu Wang, Yinghong Zhang, Zhiqiang Wang. Efficient Definitive Endoderm Differentiation from Human Parthenogenetic Embryonic Stem Cells Induced by Activin A and Wnt3a. Annals of clinical and laboratory science. 2020 Jul; 50(4):468-473. doi: ". [PMID: 32826243]
  • Nikolaos Perakakis, Alexander Kokkinos, Natia Peradze, Nikolaos Tentolouris, Wael Ghaly, Dimitrios Tsilingiris, Andreas Alexandrou, Christos S Mantzoros. Metabolic regulation of activins in healthy individuals and in obese patients undergoing bariatric surgery. Diabetes/metabolism research and reviews. 2020 07; 36(5):e3297. doi: 10.1002/dmrr.3297. [PMID: 32026536]
  • Heba Naseem, John Dreixler, Ariel Mueller, Avery Tung, Rohin Dhir, Rachna Chibber, Abid Fazal, Joey P Granger, Bhavisha A Bakrania, Victoria deMartelly, Sarosh Rana, Sajid Shahul. Antepartum Aspirin Administration Reduces Activin A and Cardiac Global Longitudinal Strain in Preeclamptic Women. Journal of the American Heart Association. 2020 06; 9(12):e015997. doi: 10.1161/jaha.119.015997. [PMID: 32495688]
  • Lykke Sylow, Birgitte F Vind, Rikke Kruse, Pauline M Møller, Jørgen F P Wojtaszewski, Erik A Richter, Kurt Højlund. Circulating Follistatin and Activin A and Their Regulation by Insulin in Obesity and Type 2 Diabetes. The Journal of clinical endocrinology and metabolism. 2020 05; 105(5):. doi: 10.1210/clinem/dgaa090. [PMID: 32112102]
  • Seong Son, Seung Hwan Yoon, Moon Hang Kim, Xiang Yun. Activin A and BMP chimera (AB204) induced bone fusion in osteoporotic spine using an ovariectomized rat model. The spine journal : official journal of the North American Spine Society. 2020 05; 20(5):809-820. doi: 10.1016/j.spinee.2019.12.015. [PMID: 31899374]
  • Juuso Paajanen, Ilkka Ilonen, Helena Lauri, Tommi Järvinen, Eva Sutinen, Hely Ollila, Eeva Rouvinen, Karl Lemström, Jari Räsänen, Olli Ritvos, Katri Koli, Marjukka Myllärniemi. Elevated Circulating Activin A Levels in Patients With Malignant Pleural Mesothelioma Are Related to Cancer Cachexia and Reduced Response to Platinum-based Chemotherapy. Clinical lung cancer. 2020 05; 21(3):e142-e150. doi: 10.1016/j.cllc.2019.10.013. [PMID: 31734071]
  • Alexandra L Thomas, Karla Castellanos, Georgina Mancinelli, Yinglin Xia, Jessica Bauer, Cemal Yazici, Giamila Fantuzzi, Rosa F Hwang, Nancy L Krett, Georgios I Papachristou, David C Whitcomb, Barbara Jung. Activin A Modulates Inflammation in Acute Pancreatitis and Strongly Predicts Severe Disease Independent of Body Mass Index. Clinical and translational gastroenterology. 2020 05; 11(5):e00152. doi: 10.14309/ctg.0000000000000152. [PMID: 32358238]
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